# FDA recall Z-1144-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-04-21.

## Product

Effluent Sample Bag

## Reason for recall

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

## Distribution

US Nationwide distribution in the states of CA, MO, MA, AZ, TX, FL, NY, MD, OH.

## Key facts

- **Recall number:** Z-1144-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-21
- **Report date:** 2022-06-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1144-2022

## Citation

> AI Analytics. FDA recall Z-1144-2022. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-1144-2022. Source: US FDA. Licensed CC0.

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